Canonical Allele Identifier: PA309588
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202559

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Pro10015Ala
CA309587
NM_001256850.1:c.30043C>G